Medical Device Recall: Medfusion Syringe Pumps

The Food and Drug Administration (FDA) has announced a Class I recall of certain Smiths Medical Syringe Pumps due to a risk of medication delivery errors.Smiths Medical is recalling specific software versions of the Medfusion 3500 and 4000 Syringe Pumps because of a...

FDA Issues EUA for Convalescent Plasma

On August 23, 2020, the Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for convalescent plasma for the treatment of COVID-19. Based on scientific evidence available, the FDA determined that it is reasonable to believe that COVID-19...